Autosomal recessive nonsyndromic hearing loss 93

Synonyms: Deafness, autosomal recessive 93

Summary

Autosomal recessive deafness-93 is characterized by moderate to severe prelingual deafness and a distinctive U-shaped audiogram (Tabatabaiefar et al., 2011). [from OMIM]

Available tests

10 tests are in the database for this condition.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

CABP2
28 tests
Also known as: DFNB93, CABP2
Summary: calcium binding protein 2

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Hearing impairment
  Hearing impairment
  - MedGen UID: 235586
  - Concept ID: C1384666
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

Reviews

Clinical resources

Molecular resources

Consumer resources

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